BEUDAMED
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    LKY

    FDA UDI
    Qingdao Likangyuan Medical Device Co.,Ltd.·06972535040001·

    MEDICAL VACUUM PUMP

    FDA Adverse Event
    Malfunction ·DR. JOEL KAPLAN INC·Product code LKY·May 30, 2014

    ENCORE VTU-1

    FDA Adverse Event
    Injury ·ENCORE, DIV. OF WETOO, INC.·Product code LKY·August 22, 2000

    ESTEEM MANUAL

    FDA Adverse Event
    Injury ·POS-T-VAC MEDICAL·Product code LKY·November 1, 2018

    ERECAID ESTEEM VACUUM ERECTION SYSTEM

    FDA Adverse Event
    Injury ·TIMM MEDICAL TECHNOLOGIES, INC.·Product code LKY·November 17, 2006

    APEX XTENDER

    FDA Adverse Event
    Injury ·UNKNOWN·Product code LKY·May 11, 2023

    HERCULES NIGHT RIDER

    FDA Adverse Event
    Injury ·UNK·Product code LKY·August 16, 2022

    DUREX ANILLO DE PLACER

    FDA Adverse Event
    Injury ·RECKITT BENCKISER HEALTHCARE INT. LIMITED·Product code LKY·August 7, 2018

    GIDDY

    FDA Adverse Event
    GIDDY HOLDINGS, INC.·Product code LKY·February 27, 2023

    PENILE INSERTION DEVICE

    FDA Adverse Event
    Injury ·AMA - COLOPLAST CORP.·Product code LKY·October 31, 2016

    VIAGRA

    FDA Adverse Event
    Injury ·ENCORE·Product code LKY·September 23, 2008

    RESTOREX

    FDA Adverse Event
    Malfunction ·PATHRIGHT MEDICAL, INC.·Product code LKY·May 15, 2026

    RESTOREX

    FDA Adverse Event
    Injury ·PATHRIGHT MEDICAL, INC.·Product code LKY·May 15, 2026

    *

    FDA Adverse Event
    AUGUSTA MEDICAL SYSTEMS, LLC·Product code LKY·August 26, 2005

    BATHMATE

    FDA Adverse Event
    Injury ·DX PRODUCT LTD·Product code LKY·July 22, 2013

    DUREX PLEASURE RING

    FDA Adverse Event
    Injury ·RECKITT BENCKISER HEALTHCARE INT LIMITED·Product code LKY·May 18, 2017

    POSAT-T-VAC PUMP

    FDA Adverse Event
    Injury ·POS-T-VAC INC.·Product code LKY·June 13, 2018

    EXTERNAL PENILE RIGIDITY

    FDA Adverse Event
    Injury ·AUGUSTA MEDICAL SYSTEMS·Product code LKY·May 2, 2017

    Antisera, Fluorescent, Chlamydia Spp.

    FDA classification
    FDA Class 1 ·Antisera, Fluorescent, Chlamydia Spp.

    Device, External Penile Rigidity

    FDA classification
    FDA Class 2 ·Device, External Penile Rigidity